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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114922Generated: October 31, 2026

3-Chlorothiophene-2-carbonyl chloride → 3-(4-Aminopyrimidin-5-yl)-5-(3-chloro-thiophen-2-yl)-[1,2,4]-oxadiazole

https://huagongshe.com/reaction/2114922

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorothiophene-2-carbonyl chlorideHCID 2735824—
Reactant4-Amino-pyrimidine-5-amidoximeHCID 2740355—
Product3-(4-Aminopyrimidin-5-yl)-5-(3-chloro-thiophen-2-yl)-[1,2,4]-oxadiazoleHCID 9814247—

Reaction Steps

The title compound was prepared from 4-amino-pyrimidine-5-amidoxime (50 mg, 0.33 mmol) and 3-chloro-thiophene-2-carbonyl chloride (59 mg, 0.33 mmol), similar to Example 16, and yielded 25 mg (27%) of yellow solid. 1H NMR (CDCl3): 9.18 (s, 1H), 8.69 (s, 1H), 7.66 (d, J=5.22 Hz, 1H), 7.16 (d, J=5.22 Hz, 1H), 5.85 (s, 1H), 3.51 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435750B2
Source datasetuspto-grants-2008_10
ORD IDord-a825870d4c5a48f7be365e6a6d876a94
Source noteuspto-grants-2008_10